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Compound Detail

CHEMBL414029

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CC[C@H](C)[C@H](NC(=O)[C@H](C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](N)CCCNC(=N)N)C(=O)N[C@@H](CC(C)C)C(=O)O

Basic Information

ChEMBL ID CHEMBL414029
Phase Preclinical
Structure Type BOTH
InChI Key DARTXRMMBXCPJL-YLUGYNJDSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

888.1
MW (Da)
-1.60
ALogP
11
HBA
14
HBD
373.2
PSA (Ų)
0.03
QED
3
Ro5 Violations
26
Rot. Bonds

Drug Information

Molecule Type Protein
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C41H69N13O9
MW 888.08
Aromatic Rings 1
Heavy Atoms 63
NP-Likeness 0.12

Activity Summary

Ki 1 meas. best 8.17

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
Ki 8.17 8.17 6.8 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked Ki = 6.8 nM 8.17 Displacement of [3H]neurotensin from pig NTR1 18276136

Literature References

PubMed DOI Target Context # Activities
18276136 10.1016/j.bmcl.2008.01.110 Unchecked 1
18276136 10.1016/j.bmcl.2008.01.110 Neurotensin receptor type 1 1

Data from ChEMBL 36 via Core Engine